Pallister-Hall Syndrome Details

Expanded Description

Pallister-Hall Syndrome [PHS] is a multiple-anomaly rare genetic disorder caused by mutations in the GLI3 gene, short arm of the 7th Chromosome.

Primary diagnostic features of PHS include: Hypothalamic Hamartoma [HH] of the Hypothalamus; Bifid Epiglottis; Syndactyly; Polydactyly and Gelastic ‘Seizures’.

Prevalence

No prevalence information has been added yet.

Causes

Autosomal dominant.

Disorder Symptoms

No symptom information has been added yet.

We don't have any symptoms yet.

Diagnosis

No diagnosis information has been added yet.

Diagnostic Tests

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We don't have any tests yet.

Disorder Treatments

No treatment information has been added yet

We don't have any treatments yet.

Prognosis

No prognosis information has been added yet

Tips for Living with the Disorder

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